Complement control protein factor H: the good, the bad, and the inadequate

VP Ferreira, MK Pangburn, C Cortés - Molecular immunology, 2010 - Elsevier
The complement system is an essential component of the innate immune system that
participates in elimination of pathogens and altered host cells and comprises an essential …

The human complement factor H: functional roles, genetic variations and disease associations

SR de Córdoba, J Esparza-Gordillo, EG de Jorge… - Molecular …, 2004 - Elsevier
Factor H is an essential regulatory protein that plays a critical role in the homeostasis of the
complement system in plasma and in the protection of bystander host cells and tissues from …

[HTML][HTML] Genetic studies into inherited and sporadic hemolytic uremic syndrome

P Warwicker, THJ Goodship, RL Donne, Y Pirson… - Kidney international, 1998 - Elsevier
Genetic studies into inherited and sporadic hemolytic uremic syndrome. Hemolytic uremic
syndrome (HUS) in adults carries a high morbidity and mortality, and its cause remains …

Anti–factor H autoantibodies associated with atypical hemolytic uremic syndrome

C Loirat, S Cloarec, MA Macher, J Blouin… - Journal of the …, 2005 - journals.lww.com
Several studies have demonstrated genetic predisposition in non–shigatoxin-associated
hemolytic uremic syndrome (HUS), involving regulatory proteins of the complement …

Hijacking factor H for complement immune evasion

SR Moore, SS Menon, C Cortes… - Frontiers in …, 2021 - frontiersin.org
The complement system is an essential player in innate and adaptive immunity. It consists of
three pathways (alternative, classical, and lectin) that initiate either spontaneously …

A Novel Sialic Acid Binding Site on Factor H Mediates Serum Resistance of Sialylated Neisseria gonorrhoeae

S Ram, AK Sharma, SD Simpson, S Gulati… - The Journal of …, 1998 - rupress.org
Factor H (fH), a key alternative complement pathway regulator, is a cofactor for factor I–
mediated cleavage of C3b. fH consists of 20 short consensus repeat (SCR) domains. Sialic …

Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H

SR De Córdoba, EG De Jorge - Clinical & Experimental …, 2008 - academic.oup.com
Summary OTHER ARTICLES PUBLISHED IN THIS TRANSLATIONAL MINI-REVIEW
SERIES ON COMPLEMENT FACTOR H Structural and functional correlations for factor H …

On phagocytes and macular degeneration

X Guillonneau, CM Eandi, M Paques, JA Sahel… - Progress in retinal and …, 2017 - Elsevier
Age related macular degeneration (AMD) is a complex multifactorial disease caused by the
interplay of age and genetic and environmental risk factors. A common feature observed in …

The complement regulator factor H binds to the surface protein OspE of Borrelia burgdorferi

J Hellwage, T Meri, T Heikkilä, A Alitalo… - Journal of Biological …, 2001 - ASBMB
Spirochete bacteria of the Borrelia burgdorferi sensu lato complex cause Lyme borreliosis.
The three pathogenic subspecies Borrelia garinii, Borrelia afzelii, and Borrelia burgdorferi …

Dual interaction of factor H with C3d and glycosaminoglycans in host–nonhost discrimination by complement

T Kajander, MJ Lehtinen, S Hyvärinen… - Proceedings of the …, 2011 - National Acad Sciences
The alternative pathway of complement is important in innate immunity, attacking not only
microbes but all unprotected biological surfaces through powerful amplification. It is …